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多西他赛化疗用于转移性激素难治性前列腺癌的一线姑息化疗及后续再治疗:伯明翰经验

Docetaxel chemotherapy for metastatic hormone refractory prostate cancer as first-line palliative chemotherapy and subsequent re-treatment: Birmingham experience.

作者信息

Ansari Jawaher, Hussain Syed Anwer, Zarkar Anjali, Tanguay Jacob S, Bliss Julie, Glaholm John

机构信息

University Hospital Birmingham NHS Trust, Metchley Drive, Birmingham, UK.

出版信息

Oncol Rep. 2008 Oct;20(4):891-6.

Abstract

Three-weekly docetaxel chemotherapy with prednisolone is now considered standard of care for patients with metastatic hormone refractory prostate cancer (MHRPC). This study reports the efficacy and toxicity of first-line docetaxel chemotherapy followed subsequently by re-treatment on biochemical disease progression (BDP). Forty-two patients with MHRPC were treated with three-weekly docetaxel chemotherapy 75 mg/m(2) and 10 mg of prednisolone daily. Median age 73 years (range 58-87) and median initial PSA 182 ng/ml (range 19.9-1500). Of these patients, 10 were re-treated with the same regimen (second-line chemotherapy) on BDP. A further 3 out of these 10 patients received 2nd re-treatment (third-line chemotherapy) with docetaxel chemotherapy on BDP. Fifty-four percent of patients responded to first-line docetaxel chemotherapy and all re-treated patients responded again with a PSA reduction >50%. Median treatment-free interval prior to second and third-line chemotherapy was 24 and 26 weeks, respectively. Grade 3 or 4 neutropenia occurred in 2.5, 7 and 12% of the total number of cycles in patients receiving first-, second- and third-line docetaxel chemotherapy, respectively. Median survival was 13 months (range 3-35) and one-year overall survival 52%. This is the first report of three-weekly docetaxel chemotherapy re-treatment in patients with MHRPC and demonstrates that patients who initially respond to docetaxel chemotherapy maintain their sensitivity to subsequent re-treatment without a significant rise in haematological toxicity.

摘要

对于转移性激素难治性前列腺癌(MHRPC)患者,三周一次的多西他赛联合泼尼松化疗目前被视为标准治疗方案。本研究报告了一线多西他赛化疗的疗效和毒性,随后在生化疾病进展(BDP)时进行再治疗的情况。42例MHRPC患者接受三周一次的多西他赛化疗,剂量为75mg/m²,每日联合10mg泼尼松。中位年龄73岁(范围58 - 87岁),初始前列腺特异抗原(PSA)中位值为182ng/ml(范围19.9 - 1500)。其中10例患者在BDP时接受相同方案的再治疗(二线化疗)。这10例患者中的另外3例在BDP时接受了多西他赛化疗的第二次再治疗(三线化疗)。54%的患者对一线多西他赛化疗有反应,所有接受再治疗的患者PSA再次下降>50%。二线和三线化疗前的中位无治疗间隔分别为24周和26周。接受一线、二线和三线多西他赛化疗的患者,3/4级中性粒细胞减少分别发生在总疗程的2.5%、7%和12%。中位生存期为13个月(范围3 - 35个月),一年总生存率为52%。这是关于MHRPC患者三周一次多西他赛化疗再治疗的首次报告,表明最初对多西他赛化疗有反应的患者对后续再治疗保持敏感性,且血液学毒性无显著增加。

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